27 results
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D1.418 - An EBP Gene Variant in a Child with Immunodeficiency: A Case from the Chondrodysplasia Pontata Spectrum

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D1.419 - The management of Immunological Diseases in Internal Medicine Departments

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D1.404 - Live Renal Transplantation Outcome in Egyptian Cohort: A Single Center Study

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D1.405 - Establishment of a Mouse Nasal Epithelial Cell Air–Liquid Interface Culture System and Its Application in Mucosal Barrier Research

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D1.407 - Real-world patient characterization, prior long-term prophylactic prescribing patterns, and treatment outcomes for adults on berotralstat with hereditary angioedema in Japan

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D1.413 - A Novel Variant of CORO1A Gene Contributing to The Development of Primary Immunodeficiency in Children

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D1.415 - Regulatory T‑Cell Deficiency and NF‑κB/IL‑1β Activation in Dilated Cardiomyopathy

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D1.472 - Features of the intestinal microbiota composition in infants with allergy: comparison of two diagnostic methods

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D1.473 - Features of the intestinal microbiota composition in infants with IgE- and non-IgE-mediated allergy

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D1.476 - Impact of neonatal vaccination on the incidence of atopic dermatitis in children by 36 months: a prospective cohort study

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D1.480 - Polysomnographic phenotypes of sleep-disordered breathing in children with asthma: a systematic review

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D1.467 - Economic Burden of Allergic Diseases in Children: Global Evidence and Implications for Kyrgyzstan

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D1.475 - Significance of air-trapping and pulmonary hyperinflation in the severity of broncho-obstructive manifestations in children with cystic fibrosis

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D1.478 - Hyper-IgE in allergic bronchopulmonary aspergillosis: diagnostic challenges

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D1.479 - Lung function in children with cystic fibrosis associated with wheezing

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D2.44 - Subjective assessment of sleep quality in adult patients with hereditary angioedema

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D2.47 - Unmasking Melkersson-Rosenthal Syndrome: Diagnostic Challenges in a Patinent Pressenting With Angioedema

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D2.43 - Hereditary Angioedema Can Hit at Any Age: A Case Report in Egypt

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D2.45 - Fixed Drug Eruption Due to Fenofibrate Hypersensitivity

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D2.46 - Patient with the overlap of Hereditary angioedema and Chronic spontaneous urticaria